Canonical Allele Identifier: CA603247976
Gene: CD69 HGNC NCBI

Linked Data

dbSNP Id: rs1456301018
gnomAD v2: 12-9910193-AC-A
gnomAD v3: 12-9757597-AC-A
gnomAD v4: 12-9757597-AC-A
MyVariant Identifiers: chr12:g.9910194del (hg19) chr12:g.9757598del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9757598del , CM000674.2:g.9757598del GRCh38
NC_000012.11:g.9910194del , CM000674.1:g.9910194del GRCh37
NC_000012.10:g.9801461del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000228434.7:c.65-1179del MANE Select ENSP00000228434.3:n.65-1179del
ENST00000416624.6:n.146-1179del
ENST00000536709.1:c.65-1179del ENSP00000442597.1:n.65-1179del
ENST00000543147.1:n.146-1179del
NM_001781.2:c.65-1179del MANE Select NP_001772.1:n.65-1179del
Search 100 bp 5'
Search 100 bp 3'